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心力衰竭患者外周血管张力的调节:血管紧张素II的作用

Regulation of peripheral vascular tone in patients with heart failure: contribution of angiotensin II.

作者信息

Newby D E, Goodfield N E, Flapan A D, Boon N A, Fox K A, Webb D J

机构信息

Clinical Pharmacology Unit, University of Edinburgh, Western General Hospital, UK.

出版信息

Heart. 1998 Aug;80(2):134-40. doi: 10.1136/hrt.80.2.134.

Abstract

OBJECTIVE

To determine directly the contribution of angiotensin II to basal and sympathetically stimulated peripheral arteriolar tone in patients with heart failure.

DESIGN

Parallel group comparison.

SUBJECTS

Nine patients with New York Heart Association grade II-IV chronic heart failure, and age and sex matched controls.

INTERVENTIONS

Forearm plethysmography, lower body negative pressure, local intra-arterial administration of losartan, angiotensin II, and noradrenaline, and estimation of plasma hormone concentrations.

MAIN OUTCOME MEASURES

Forearm blood flow responses, plasma hormone concentrations.

RESULTS

Baseline blood pressure, heart rate, and forearm blood flow did not differ between patients and controls. In comparison with the non-infused forearm, losartan did not affect basal forearm blood flow (95% confidence interval -5.5% to +7.3%) or sympathetically stimulated vasoconstriction in controls. However, the mean (SEM) blood flow in patients increased by 13(5)% and 26(7)% in response to 30 and 90 micrograms/min of losartan respectively (p < 0.001). Lower body negative pressure caused a reduction in forearm blood flow of 20(5)% in controls (p = 0.008) and 13(5)% (p = 0.08) in patients (p = 0.007, controls v patients). Blood flow at 90 micrograms/min of losartan correlated with plasma angiotensin II concentration (r = 0.77; p = 0.03). Responses to angiotensin II and noradrenaline did not differ between patients and controls.

CONCLUSIONS

Losartan causes acute local peripheral arteriolar vasodilation in patients with heart failure but not in healthy control subjects. Endogenous angiotensin II directly contributes to basal peripheral arteriolar tone in patients with heart failure but does not augment sympathetically stimulated peripheral vascular tone.

摘要

目的

直接确定血管紧张素II对心力衰竭患者基础状态下及交感神经刺激引起的外周小动脉张力的影响。

设计

平行组比较。

研究对象

9例纽约心脏协会II-IV级慢性心力衰竭患者,以及年龄和性别匹配的对照组。

干预措施

前臂体积描记法、下体负压、局部动脉内给予氯沙坦、血管紧张素II和去甲肾上腺素,并测定血浆激素浓度。

主要观察指标

前臂血流反应、血浆激素浓度。

结果

患者与对照组的基线血压、心率和前臂血流无差异。与未输注药物的前臂相比,氯沙坦对对照组的基础前臂血流(95%置信区间为-5.5%至+7.3%)或交感神经刺激引起的血管收缩无影响。然而,在患者中,分别给予30微克/分钟和90微克/分钟氯沙坦后,平均(标准误)血流分别增加了13(5)%和26(7)%(p<0.001)。下体负压使对照组前臂血流减少20(5)%(p=0.008),使患者前臂血流减少13(5)%(p=0.08)(p=0.007,对照组与患者组比较)。氯沙坦剂量为90微克/分钟时的血流与血浆血管紧张素II浓度相关(r=0.77;p=0.03)。患者与对照组对血管紧张素II和去甲肾上腺素的反应无差异。

结论

氯沙坦可使心力衰竭患者发生急性局部外周小动脉血管舒张,但对健康对照者无此作用。内源性血管紧张素II直接影响心力衰竭患者的基础外周小动脉张力,但不增强交感神经刺激引起的外周血管张力。

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